Canonical Allele Identifier: CA400667462

Gene: RGS9

Linked Data

• MyVariant Identifiers: chr17:g.63193284T>G (hg19) ; chr17:g.65197166T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65197166T>G , CM000679.2:g.65197166T>G	GRCh38
NC_000017.10:g.63193284T>G , CM000679.1:g.63193284T>G	GRCh37
NC_000017.9:g.60623746T>G	NCBI36
NG_013021.1:g.64829T>G
NG_013021.2:g.64829T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262406.10:c.901T>G MANE Select	ENSP00000262406.9:p.Phe301Val
ENST00000635833.1:c.901T>G	ENSP00000490658.1:p.Phe301Val
ENST00000262406.9:c.901T>G	ENSP00000262406.9:p.Phe301Val
ENST00000443584.7:c.892T>G	ENSP00000405814.3:p.Phe298Val
ENST00000449996.7:c.892T>G	ENSP00000396329.3:p.Phe298Val
ENST00000577595.1:n.829T>G
ENST00000581175.5:n.909T>G
ENST00000584234.5:c.901T>G	ENSP00000463410.1:p.Phe301Val
NM_001081955.2:c.892T>G	NP_001075424.1:p.Phe298Val
NM_001165933.1:c.892T>G	NP_001159405.1:p.Phe298Val
NM_003835.3:c.901T>G	NP_003826.2:p.Phe301Val
XM_011525426.1:c.313T>G	XP_011523728.1:p.Phe105Val
XM_011525426.3:c.313T>G	XP_011523728.1:p.Phe105Val
NM_003835.4:c.901T>G MANE Select	NP_003826.2:p.Phe301Val
NM_001081955.3:c.892T>G	NP_001075424.1:p.Phe298Val
NM_001165933.2:c.892T>G	NP_001159405.1:p.Phe298Val